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Merck
CN

776505

4-羟基苄胺

别名:

4-(氨甲基)苯酚

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关于此项目

经验公式(希尔记法):
C7H9NO
化学文摘社编号:
分子量:
123.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Form:
solid
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form

solid

Quality Level

mp

123-128 °C

functional group

amine

SMILES string

NCc1ccc(O)cc1

InChI

1S/C7H9NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H,5,8H2

InChI key

RQJDUEKERVZLLU-UHFFFAOYSA-N



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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C Hartmann et al.
Biochemistry, 32(9), 2234-2241 (1993-03-09)
Anaerobic, rapid-scanning stopped-flow spectroscopy has been used to investigate the UV-visible absorbance changes (300-540 nm) that occur in the spectrum of bovine serum amine oxidase during reduction by benzylamine, p-hydroxybenzylamine, and p-methoxybenzylamine. The reaction of enzyme with benzylamine generates detectable
Qichen Zhan et al.
Small (Weinheim an der Bergstrasse, Germany), 15(3), e1803926-e1803926 (2018-11-30)
Controlled drug release systems can enhance the safety and availability but avoid the side effect of drugs. Herein, the concept of DNA complementary base pairing rules in biology is used to design and prepare a photothermal-triggered drug release system. Adenine
P R Williamson et al.
The Journal of biological chemistry, 261(20), 9477-9482 (1986-07-15)
The catalysis of amine oxidation by lysyl oxidase has been probed to assess for the likely order of substrate binding and product release and to discriminate between mechanistic alternatives previously proposed for other copper-dependent amine oxidases using molecular oxygen as



全球贸易项目编号

货号GTIN
776505-5G04061832940403
776505-25G04061832940397